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Fda Cvm Jobs (NOW HIRING)

Sr Research Scientist

Indianapolis, IN · Hybrid

$94K - $120K/yr

Extensive knowledge of current quality and regulatory requirements for new drug products and a demonstrated track record of successful interactions with regulatory agencies (e.g., FDA/CVM, EMA) on ...

Guide the design and development of the global regulatory strategy for development projects, with a primary focus on CVM/FDA submissions. * Serve as the dedicated regulatory subject matter expert on ...

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Fda Cvm information

What is the FDA CVM?

The FDA Center for Veterinary Medicine (CVM) is a branch of the U.S. Food and Drug Administration responsible for regulating animal drugs, animal food (including pet food), and veterinary medical devices. CVM ensures that these products are safe, effective, and properly labeled for animals and the people who handle or consume animal products. The center works closely with veterinarians, pet owners, farmers, and industry representatives to protect both animal and human health.

What are the key skills and qualifications needed to thrive as an FDA Center for Veterinary Medicine (CVM) professional?

To thrive as a professional at the FDA Center for Veterinary Medicine (CVM), you need a solid background in veterinary medicine, biology, or a related scientific field, often supported by advanced degrees such as a DVM, PhD, or equivalent. Familiarity with regulatory review systems, data analysis software, and knowledge of FDA regulations and guidance documents is crucial. Excellent analytical thinking, attention to detail, and strong written and verbal communication skills distinguish top performers in this role. These competencies ensure rigorous safety evaluations, effective regulatory oversight, and clear communication of scientific decisions impacting animal and public health.

What are some common challenges faced by professionals working at the FDA Center for Veterinary Medicine (CVM)?

Professionals at the FDA CVM often face the challenge of balancing regulatory compliance with evolving scientific advancements in animal health. Staying updated on complex regulations, interpreting scientific data, and ensuring timely evaluations of animal drugs and feed additives are integral to the role. Collaborating across multidisciplinary teams—such as veterinarians, toxicologists, and policy experts—can require strong communication and project management skills. Managing workload during high-priority reviews or responding to emerging animal health concerns also adds to the dynamic nature of the work.
More about Fda Cvm jobs
Infographic showing various Fda Cvm job openings in the United States as of August 2026, with employment types broken down into 81% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution.

Sr Research Scientist

Elanco

Indianapolis, IN • Hybrid

$94K - $120K/yr

Full-time

Retirement, PTO

Re-posted 11 days ago


Elanco rating

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical


Job description

At Elanco (NYSE: ELAN) - it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals' lives better makes life better - join our team today!

Your Role:

As a Senior Research Scientist in Analytical Development, you will be a key scientific leader on our Technical Development (TD) team, directly contributing to Elanco's mission by advancing the analytical and dissolution control strategies for our small molecule portfolio. In this role, you will be responsible for supporting our drug development pipeline through a diverse range of analytical activities, ensuring our new animal health products meet global quality and regulatory standards.

Your Responsibilities:

  • Develop, validate, and deliver robust analytical and dissolution methods and specifications, while driving the evaluation and implementation of new technologies to advance our drug development process.

  • Interpret complex scientific data, draw relevant conclusions, and effectively report and present technical results to internal teams and at external scientific conferences.

  • Author and support the generation of international registration documents, partnering with manufacturing and regulatory colleagues to drive drug product commercialization and technical submissions to global health authorities.

  • Mentor and coach emerging technical talent within the analytical development function, fostering a culture of scientific excellence.

  • Ensure all activities are compliant with internal and external quality standards and guidelines, including GxP, SOPs, and HSE.

What You Need to Succeed (minimum qualifications):

  • Education: PhD in Analytical Chemistry, Pharmacy, Pharmaceutical Sciences, or a related field with a minimum of 5 years of experience in pharmaceutical development; M.S. in a related field with a minimum of 10 years of experience; or B.S. in a related field with a minimum of 15 years of experience.

  • Experience: Strong expertise in chromatographic (HPLC/UPLC), spectroscopic (UV/VIS), and dissolution method development (specifically with USP Apparatus II and IV).

  • Top 2 skills: Extensive knowledge of current quality and regulatory requirements for new drug products and a demonstrated track record of successful interactions with regulatory agencies (e.g., FDA/CVM, EMA) on analytical topics.

What will give you a competitive edge (preferred qualifications):

  • Significant experience in dissolution development and regulatory submissions.

  • Experience with mass spectrometry (MS) and other areas of analytical method development.

  • Proven scientific leadership skills combined with strong problem-solving and creative thinking abilities.

  • Demonstrated ability to collaborate and positively impact interdisciplinary and international teams.

  • Experience working in regulated environments (e.g., GMP).

Additional Information:

  • Travel: 10%

  • Location: Global Elanco Headquarters - Indianapolis, IN - Hybrid Work Environment

Don't meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!

Elanco Benefits and Perks:

We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:

  • Multiple relocation packages

  • Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)

  • 8-week parental leave

  • 9 Employee Resource Groups

  • Annual bonus offering

  • Flexible work arrangements

  • Up to 6% 401K matching

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against jobrelated criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.


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